Compensatory growth is widespread in juvenile animals; it refers to the ability to grow at faster-than-routine rates, following intervals of slow growth due to reduced food supply or temperature. Whether the ability to grow rapidly under routine conditions is associated with enhanced or reduced compensatory growth performance is unknown. We examine the among-population covariance in routine and compensatory growth ability in juvenile Atlantic silverside, Menidia menidia. Routine growth rate in this species positively varies with latitude, indicating selection for more rapid increase in size in highly seasonal environments. High-latitude fish may also show strong compensatory ability, considering the selective value of rapid recovery from winter for growth and breeding in the spring. Alternatively, low-latitude fish may be more readily able to compensate because they have more energetic scope for growth. To test these alternatives, laboratory-reared juveniles from three populations [Nova Scotia (NS), New York (NY), and South Carolina (SC)] were maintained at temperatures promoting maximum growth. In each population, control fish were furnished ad libitum rations, while treatment fish were subject to 5 or 10 days of maintenance ration before returning to unlimited ration. Treatment fish grew slightly in length, but not mass, over the period of limited ration. We observed compensatory growth in all populations. NS fish recovering from 10 days of limited ration grew 12% faster in length and 46% faster in dry mass than NS control fish, over 15 days of unrestricted growth. In contrast, recovering SC fish grew 1.4% faster in length and 22% faster in dry mass than SC control fish. A period of starvation (mass loss) is not a required condition for a compensatory response, as has been assumed in theoretical work. The positive covariance between routine and compensatory growth performance indicates that the growth rate strategy of high latitude fish includes rapid recovery from periods of depletion, adding to the suite of characteristics that have differentiated along an environmental gradient in seasonality.
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Front Endocrinol (Lausanne)
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Department and Clinic of Endocrinology, Diabetes and Isotope Therapy, Wroclaw Medical University, Wrocław, Poland.
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College of Fisheries, Hubei Hongshan Laboratory/Key Lab of Freshwater Animal Breeding, Ministry of Agriculture and Rural Affairs/Engineering Research Center of Green Development for Conventional Aquatic Biological Industry in the Yangtze River Economic Belt, Ministry of Education, Huazhong Agricultural University, No. 1 Shizishan Street, Hongshan District, Wuhan, 430070, Hubei, China.
Background: Intermuscular bones (IBs) are segmental intramembranous ossifications located within myosepta. They share similarities with tendon ossification, a form of heterotopic ossification (HO). The mechanisms underlying IB formation remain incompletely understood.
View Article and Find Full Text PDFCell Biol Toxicol
December 2024
Department of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Environmental chemicals and toxins are known to impact human health and contribute to cancer developments. Among these, genotoxins induce genetic mutations critical for cancer initiation. In the liver, proliferation serves not only as a compensatory mechanism for tissue repair but also as a potential risk factor for the progression of premalignant lesions.
View Article and Find Full Text PDFThyroid
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National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), Bethesda, Maryland, USA.
Thyroid hormones (TH) play a key role in fetal brain development. While severe thyroid dysfunction, has been shown to cause neurodevelopmental and reproductive disorders, the rising levels of TH-disruptors in the environment in the past few decades have increased the need to assess effects of subclinical (mild) TH insufficiency during gestation. Since embryos do not produce their own TH before mid-gestation, early development processes rely on maternal production.
View Article and Find Full Text PDFCancer Commun (Lond)
December 2024
Department of Biomedical Engineering, Department of Electrical and Computer Engineering, Photonics Center, Boston University, Boston, Massachusetts, USA.
Background: Adaptative desaturation in fatty acid (FA) is an emerging hallmark of cancer metabolic plasticity. Desaturases such as stearoyl-CoA desaturase (SCD) and fatty acid desaturase 2 (FADS2) have been implicated in multiple cancers, and their dominant and compensatory effects have recently been highlighted. However, how tumors initiate and sustain their self-sufficient FA desaturation to maintain phenotypic transition remains elusive.
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